ID

16347

Description

Protocol for Women at Increased Risk of Developing Breast Cancer; ODM derived from: https://clinicaltrials.gov/show/NCT00291135

Lien

https://clinicaltrials.gov/show/NCT00291135

Mots-clés

  1. 11/07/2016 11/07/2016 -
Téléchargé le

11 juillet 2016

DOI

Pour une demande vous connecter.

Licence

Creative Commons BY 4.0

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Eligibility Breast Cancer NCT00291135

Eligibility Breast Cancer NCT00291135

Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
evidence of hyperplasia with/without atypia upon random periareolar fine needle aspiration of breast
Description

Random Periareolar Fine-Needle Aspiration | Evidence of Breast hyperplasia | Evidence of Atypical hyperplasia of breast

Type de données

boolean

Alias
UMLS CUI [1]
C3640066
UMLS CUI [2,1]
C0332120
UMLS CUI [2,2]
C0542028
UMLS CUI [3,1]
C0332120
UMLS CUI [3,2]
C1297929
on hormone replacement therapy
Description

Hormone replacement therapy

Type de données

boolean

Alias
UMLS CUI [1]
C0282402
postmenopausal
Description

Postmenopausal state

Type de données

boolean

Alias
UMLS CUI [1]
C0232970
increased risk of developing breast cancer based on personal or family history
Description

Increased risk of breast cancer in women Due to Medical History | Increased risk of breast cancer in women Due to Family history

Type de données

boolean

Alias
UMLS CUI [1,1]
C2676211
UMLS CUI [1,2]
C0678226
UMLS CUI [1,3]
C0262926
UMLS CUI [2,1]
C2676211
UMLS CUI [2,2]
C0678226
UMLS CUI [2,3]
C0241889
never have taken aromatase inhibitors or selective estrogen receptor modulators in last six months
Description

Aromatase Inhibitors | Selective Estrogen Receptor Modulators

Type de données

boolean

Alias
UMLS CUI [1]
C0593802
UMLS CUI [2]
C0732611
women who have a high risk of breast cancer
Description

Gender | Breast Carcinoma High risk

Type de données

boolean

Alias
UMLS CUI [1]
C0079399
UMLS CUI [2,1]
C0678222
UMLS CUI [2,2]
C0332167
older than 18 years
Description

Age

Type de données

boolean

Alias
UMLS CUI [1]
C0001779
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
anticoagulants
Description

Anticoagulants

Type de données

boolean

Alias
UMLS CUI [1]
C0003280
marked breast tenderness
Description

Breast tenderness Marked

Type de données

boolean

Alias
UMLS CUI [1,1]
C0262397
UMLS CUI [1,2]
C1706089
pregnant or within twelve months of breast feeding/childbirth
Description

Pregnancy | Breast Feeding | Childbirth

Type de données

boolean

Alias
UMLS CUI [1]
C0032961
UMLS CUI [2]
C0006147
UMLS CUI [3]
C1148523

Similar models

Eligibility Breast Cancer NCT00291135

Name
Type
Description | Question | Decode (Coded Value)
Type de données
Alias
Item Group
C1512693 (UMLS CUI)
Random Periareolar Fine-Needle Aspiration | Evidence of Breast hyperplasia | Evidence of Atypical hyperplasia of breast
Item
evidence of hyperplasia with/without atypia upon random periareolar fine needle aspiration of breast
boolean
C3640066 (UMLS CUI [1])
C0332120 (UMLS CUI [2,1])
C0542028 (UMLS CUI [2,2])
C0332120 (UMLS CUI [3,1])
C1297929 (UMLS CUI [3,2])
Hormone replacement therapy
Item
on hormone replacement therapy
boolean
C0282402 (UMLS CUI [1])
Postmenopausal state
Item
postmenopausal
boolean
C0232970 (UMLS CUI [1])
Increased risk of breast cancer in women Due to Medical History | Increased risk of breast cancer in women Due to Family history
Item
increased risk of developing breast cancer based on personal or family history
boolean
C2676211 (UMLS CUI [1,1])
C0678226 (UMLS CUI [1,2])
C0262926 (UMLS CUI [1,3])
C2676211 (UMLS CUI [2,1])
C0678226 (UMLS CUI [2,2])
C0241889 (UMLS CUI [2,3])
Aromatase Inhibitors | Selective Estrogen Receptor Modulators
Item
never have taken aromatase inhibitors or selective estrogen receptor modulators in last six months
boolean
C0593802 (UMLS CUI [1])
C0732611 (UMLS CUI [2])
Gender | Breast Carcinoma High risk
Item
women who have a high risk of breast cancer
boolean
C0079399 (UMLS CUI [1])
C0678222 (UMLS CUI [2,1])
C0332167 (UMLS CUI [2,2])
Age
Item
older than 18 years
boolean
C0001779 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
Anticoagulants
Item
anticoagulants
boolean
C0003280 (UMLS CUI [1])
Breast tenderness Marked
Item
marked breast tenderness
boolean
C0262397 (UMLS CUI [1,1])
C1706089 (UMLS CUI [1,2])
Pregnancy | Breast Feeding | Childbirth
Item
pregnant or within twelve months of breast feeding/childbirth
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
C1148523 (UMLS CUI [3])

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